城市污水厂污泥的浸泡油炸

提出了一种利用餐厨废油为热交换介质,在常压下对城市污水厂污泥进行油炸干化制成固体燃料,以实现城镇两大废弃物一污泥和餐厨废油综合处置的方法。以大豆油模拟餐厨废油,研究了污泥油炸干燥特性及过程影响参数。实验结果表明,污泥经油炸干化后,干基含水率从初始的4．56kg／kg降低至0．05kg／kg,干基含油率升为0．37～0．47kg／kg,干污泥热值达到21．551～24．082MJ／kg,是一种高热值固体燃料。油温对污泥油炸干化过程影响显著,当油温从120℃升至180℃时,污泥干燥时间从28min缩短至4min。实验条件下,1t餐厨废油可处理约8．3t湿污泥。     

铁碳布空气阴极微生物燃料电池的产电性能

使用铁代替铂作为阴极催化剂,制作含铁碳布空气阴极并构建单室MFC(Fe-C-ACMFC)。以乙酸钠为燃料,通过稳态放电法和循环伏安测试等测试手段,分析了不同铁含量对Fe-C-ACMFC产电性能的影响以及性能最优Fe-C-ACM-FC的连续运行稳定性。结果表明,随着铁含量的增加,Fe-C-ACMFC启动期开路电压(OCV)逐步提高,达到峰值后,随着铁含量的增加而降低;同样,Fe-C-ACMFC极化性能和功率密度等产电性能也随铁含量的增加先升高再降低;当铁含量为0.7 mg/cm2时,MFC的产电性能最优,最大开路电压为593 mV,表观内阻为89Ω,最大功率密度达到12 907 mW/m3,并且经循环伏安测试,电池放电容量几乎没有变化,表明Fe-C-ACMFC的性能比较稳定,能够长期运行。由于铁催化剂价格远远低于铂催化剂,因此,铁碳布空气阴极MFC更利于推广应用。     

粉煤灰的改性及其对高盐苯胺废水的处理

以盐酸和硫酸作为改性剂,对粉煤灰进行改性。通过正交实验得到最佳改性粉煤灰制备条件为：V（盐酸）∶V（硫酸）=1∶5,浸泡时间6h,活化时间6h,活化温度250℃。在初始苯胺质量浓度为200mg/L、氯化钠质量分数为15%、吸附时间为60min的条件下,采用在最佳条件下制备得到的改性粉煤灰对苯胺进行吸附,吸附量可达4.16mg/g。采用Freundlich方程可更好地对改性粉煤灰吸附苯胺的过程进行拟合。     

一体式MFC-好氧MBR运行效果及膜污染特性

膜生物反应器(MBR)是一种高效的污水处理工艺,而微生物燃料电池(MFC)能利用NO-3作为电子受体进行脱氮。为解决膜生物反应器(MBR)脱氮效率低和膜污染问题,建立了一套能够进行脱氮、有效抑制膜污染的一体式MFC-好氧MBR新工艺。以开路MFC-MBR反应器为对照,对耦合系统中污水处理效果、膜污染情况进行研究。研究表明,2套系统的COD去除率均超过88%,对NH4-N的去除均达到99%。闭路MFC-MBR系统TN去除率达到69.4%,高于开路系统的55.3%。混合液的MLVSS/MLSS稳定在88%左右,同时耦合系统能够改善污泥混合液的性质,zeta电位的绝对值和粘度较开路系统有所减少,污泥颗粒平均体积粒径(233.482μm)较开路系统(94.877μm)有明显增加,膜清洗周期延长了41.17%。     

双室微生物燃料电池型BOD传感器性能

构建了双室微生物燃料电池(MFC),并应用于污水BOD的检测。优化了MFC型BOD传感器的检测条件,分析了传感器进行污水BOD检测的特征。结果表明,以A2/O污水处理工艺中厌氧段污泥进行接种,双室MFC型BOD传感器2周内完成启动,所产电流达到稳定。传感器的最佳检测条件为外接电阻500Ω,添加缓冲溶液并维持待测水样pH为7.0,添加35 mg/L的L-半胱氨酸作为吸氧剂维持阳极室厌氧环境,阴极室富氧水流量为20 mL/min。利用MFC产生的电流峰值准确检测污水水样BOD浓度,传感器检测范围为10~50 mg/L,检测时间小于3 h;利用MFC产生的电荷量准确检测污水水样BOD浓度,检测范围为10~100 mg/L,检测时间小于10 h。利用MFC电流峰值和电荷量检测污水水样BOD浓度,偏差均小于15%,传感器运行稳定,寿命较长。     

亚硝化混合菌的固定化及去除河水NH_3-N影响因素

通过比较炉渣、陶粒和沸石3种吸附基质对污染物的吸附去除效果和吸附固定微生物的效果,筛选出廉价易得的炉渣作为载体基质,同时以2%海藻酸钠(SA)和8%聚乙烯醇(PVA)混合溶液作为包埋剂,用吸附-包埋的复合方法固定具有亚硝化功能的混合微生物,并考察了该PVA-SA-炉渣小球去除河水中NH3-N的效果和影响因素。结果表明,当投加比0.45、温度30~40℃、振荡速度150 r/min和初始NH3-N浓度6 mg/L时,微生物可保持较高的活性,经4 h处理,复合固定化颗粒对河水中NH3-N去除率为80%左右。该吸附-包埋固定化方法对于去除NH3-N具有一定的实用意义,也为河流水体净化提供了新的技术参考。     

脱氮副球菌YF1微生物燃料电池生物阴极脱氮和产电

以脱氮副球菌YF1构建纯种生物阴极微生物燃料电池(microbial fuel cell,MFC)进行脱氮和产电机理的研究。研究结果发现,阴极碳氮比、pH值对产电和脱氮效率有明显影响。当MFC的阴极运行条件pH值为8.0,碳氮比为20时,运行时间15 h时,脱氮率高达100%,输出电压为150 mV。上述结果表明,微生物燃料电池运行过程中,细菌降解硝酸根的机理为将硝酸根还原为N2或者直接将其作为自身的营养物质而利用。循环伏安(CV)与扫描电镜(SEM)的结果表明,在微生物燃料电池运行中,副球菌YF1通过接触导电作为产电的电子供体。     

用混合二元酸制备混合酸二甲酯

以工业副产物混合二元酸（DBA）和甲醇为原料,用自制PW12／SiO2作催化剂制备混合酸二甲酯（DME）,确定了最佳制备条件：甲醇与DBA摩尔比为3．5,PW12／SiO2加入量（PW12／SiO2中PW12占DBA的质量分数）为2％,反应时间为4．5h,100gDBA中甲苯加入量为50mL。在此最佳条件下,DME收率为84．7％,所得DME为无色澄清液体,其中丁二酸二甲酯的质量分数为11．03％,戊二酸二甲酯的质量分数为13．88％,己二酸二甲酯的质量分数为73．79％。PW12／SiO2具有较好的稳定性和一定的重复使用性,PW12／SiO2重复使用5次时的DME收率仍大于70％。     

Uptake of Cd, Cu, Ni and Zn by the Water Hyacinth, Eichhornia Crassipes (Mart.) Solms from Pulverised Fuel Ash (PFA) Leachates and Slurries

The main solid waste product from coal-fired power stations is pulverised fuel ash (PFA), which can be enriched in toxic elements. Disposal of PFA by dry (in landfills) or wet (by slurrying) disposal methods can release these elements into the environment. Thereafter, the contaminants can be taken up by biota such as Eichhornia crassipes, a common aquatic plant, which has the ability to accumulate elements from water. This study investigates the uptake of Cd, Cu, Ni and Zn by E. crassipes grown in leachates and slurries prepared from two different PFA samples. PFA samples were obtained from Indraprastha Power Station (IPP Stn.) in New Delhi, India and the Ratcliffe-on-Soar Power Station in the UK. E. crassipes grown in PFA leachates and slurries at 1:5 and 1:50 solid:liquid (PFA:deionised water) ratios show that the plant has a very high accumulation capacity for Cd, Cu, Ni and Zn from both leachates and slurries and the uptake of these metals is stronger in the roots than in the tops of the plant. Metal accumulation, as shown by the accumulation factor (AF) values, is higher from both leachates and slurries for plants grown in the 1:50 (PFA:DIW) ratios than in the 1:5 ratios, initial metal concentrations being higher in the 1:5 ratios than in the 1:50 ratios. Lower metal accumulation in the plants grown in slurries than in leachates is related to the high turbidity of growth medium in slurries resulting in ash particles adhering to the root surfaces thus reducing the surface area of metal absorption. Eichhornia plants are able to reduce the pH of all leachates, especially the highly alkaline Ratcliffe leachates to near neutral conditions. Accumulation of Cd and Zn by the plant is higher from the lower pH IPP leachates than the Ratcliffe leachates, indicating that these metals are more soluble and bioavailable in the acidic medium. However, accumulation of Cu and Ni is independent of the pH of the leachates, indicating that other factors, such as metal species, presence of complexing agents in the growth solutions, and effects of competing metal ions may be contributory factors towards the metal uptake and accumulation by the plant.     

An economic evaluation on the purification and storage of waste hydrogen for the use of fuel cell scooters

Safe and reliable metal hydride canisters (MHCs) for the use of hydrogen storage at low pressure can be applied to supply small fuel cell vehicles or scooters with hydrogen fuel. However, greater cost-effectiveness of hydrogen gas is obviously necessary to the successful promotion of hydrogen fuel cell scooters in the market. In this study, we use the net present value (NPV) method to evaluate the feasibility of an investment project on the supply of purified hydrogen in a pulp company at Hualien, Taiwan. The purified hydrogen can be separated from waste hydrogen by using pressure swing adsorption (PSA) technology and then be stored in MHCs. Under some assumptions of improved parameters about hydrogen production cost and hydrogen gas price, the discounted payback period of hydrogen purification and storage project in our study can be less than 10 years and the unit cost of hydrogen gas can be close to the price of gasoline. Moreover, the unit cost of hydrogen gas in our study can be lower than the cost from other sources of hydrogen.